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5,510 results for “Foods”

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zenodo32/100

Supplementary material 1 from: Rosenfeld S, Marambio J, Ojeda J, Rodríguez JP, González-Wevar C, Gerard K, Contador T, Pizarro G, Mansilla A (2018) Trophic ecology of two coexisting Sub-Antarctic limpets of the genus Nacella: Spatio-temporal variation in food availability and diet composition of Nacella magellanica and N. deaurata in the Sub-Antarctic Ecoregion of Magellan . ZooKeys 738: 1-25. https://doi.org/10.3897/zookeys.738.21175

Tables S1–S11 : Explanation note: This is a DOC file with all the temporal information of the occurrence of the algae taxa in both localities, and all the information of the PERMANOVA analyzes used in this study.

opencc-zeroApr 2018View details →
zenodo32/100

Supplementary material 1 from: Biscotti N, Bonsanto D, Viscio GD (2018) The traditional food use of wild vegetables in Apulia (Italy) in the light of Italian ethnobotanical literature. Italian Botanist 5: 1-24. https://doi.org/10.3897/ib.5.22297

Tables S1, S2, S3 : Explanation note: Table S1 (Learning areas divided by territorial district), Table S2 (Wild vegetables gathered and consumed in Apulia region) and Table S3 (Wild food plants of popular use in Italy by regions (Checklist)).

opencc-zeroApr 2018View details →
zenodo32/100

Supplementary material 1 from: Zhang Z, Zang R (2018) Diversity and distribution of food plants: Implications for conservation of the critically endangered Hainan gibbon. Nature Conservation 31: 17-33. https://doi.org/10.3897/natureconservation.31.27407

Table S1 : Explanation note: Species list, abundances and characteristics of food woody plant species for Hainan gibbon sampled in young natural secondary forests (YSF, < 25 yr since disturbance), middle-aged natural secondary forests (MSF, 25–60 yr since disturbance), old natural forests (OGF, > 60 yr since disturbance) and plantation forests (PF, 20–35 yr) of tropical forest area in BNNR, Hainan Island, China. Tot fts: total number of forest types in which the species occurs.

opencc-zeroDec 2018View details →
zenodo32/100

Facial affective responses to food with friends and strangers

<p>Raw data from a study of social context and food liking. CSV files are generated by PsychoPy. ACQ files are generated by BIOPAC Acqknowledge software.</p>

opencc-by-4.0Dec 2018View details →
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Survival under conditions of variable food availability: Resource utilization and storage in the cold‐water coral Lophelia pertusa

<p>Abstract</p> <p>Cold-water coral (CWC) reefs are hotspots of biodiversity and productivity in the deep sea, but their distribution&nbsp;is limited by the availability of food, which undergoes complex local and temporal variability. We studied&nbsp;the resource utilization, metabolism, and tissue storage of CWC Lophelia pertusa during an experimentally simulated&nbsp;3-day food pulse, of 13C15N-enriched phytodetritus, followed by a 4-week food deprivation. Oxygen consumption&nbsp;(0.145 &mu;mol O2 [mmol organic carbon {OC}]&minus;1 h&minus;1), release of particulate organic matter (0.029 &mu;mol&nbsp;particulate organic carbon [POC] [mmol OC]&minus;1 h&minus;1 and 0.005 &mu;mol particulate organic nitrogen [mmol OC]&minus;1 h&minus;1),&nbsp;ammonium excretion (0.004 &mu;mol NH4&nbsp;+ [mmol OC]&minus;1 h&minus;1), tissue C and N content, and fatty acid (FA) and amino&nbsp;acid composition did not change significantly during the experiment. Metabolization of the labeled phytodetritus,&nbsp;however, underwent distinct temporal dynamics. Initially, L. pertusa preferentially used phytodetritus-derived C for&nbsp;respiration (2.2 0.36 nmol C [mmol OC]&minus;1 h&minus;1) and mucus production (0.94 0.52 nmol C [mmol OC]&minus;1 h&minus;1),&nbsp;but those tracer fluxes declined exponentially to &lt;20% within 2 weeks after feeding and then remained stable, indicating&nbsp;that the remainder of the incorporated phytodetritus had entered a tissue pool with lower turnover. Analysis&nbsp;of 13C in individual FAs revealed a mismatch between the FAs incorporated from phytodetritus and the FA requirements&nbsp;of the coral.We suggest that feeding on other resources, such as lipid-rich zooplankton, could fill this deficiency.&nbsp;A release of 10% of their total OC as respired C and POC during the 4-week food deprivation underlines the&nbsp;importance of regular food pulses for CWC reefs.&nbsp;</p>

opencc-by-4.0Feb 2019View details →
zenodo32/100

FIGURES 33–39 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 33–39. Fourth instar larva of Moiradiomus lachesis: 33, dorsal habitus view, scale bar = 0.5 mm; 34, ventral view of mouthparts, enlarged; 35, right antenna, enlarged; 36, dorsal view of right mandible, enlarged; 37, diverse dorsal setae, enlarged; 38, tibiotarsus showing distribution of clavate setae, enlarged; 39, apex of tibiotarsus (setae removed) showing shape of tarsal claw, enlarged.

opennotspecifiedFeb 2019View details →
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FIGURES 25–28 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 25–28. Diagrammatic ventral view of Moiradiomus prosterna (setae, color patterns, and surface punctation not indicated): 25, M. clotho; 26, M. lachesis; 27, M. atopos; 28, M. nanita.

opennotspecifiedFeb 2019View details →
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FIGURES 21–24 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 21–24. Dorsal view of right mandible: 21, Subcoccinella vigintiquatuorpunctata (L.) (folivorous) (after Kovář 1996); 22, Bulaea sp. (omnivorous with emphasis on pollinivory/phytophagy); 23, Moiradiomus lachesis (enlarged detail of apical portion of incisor blade shown to left of main structure) (specialized on Piper food bodies); 24, Adalia bipunctata (entomophagous with emphasis on aphids) (after Kovář 1996).

opennotspecifiedFeb 2019View details →
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FIGURES 17–20. Moiradiomus species habitus illustrations. 17, M in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 17–20. Moiradiomus species habitus illustrations. 17, M. atropos: holotype, male; 18, M. atropos: paratype, female. 19, M. nanita: holotype, male; 20, M. nanita: paratype, female. Scale bar = 0.5 mm.

opennotspecifiedFeb 2019View details →
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FIGURES 3–12 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 3–12. Genitalia of Diomini and Selvadiina (Hyperaspidini): 3–6, female genitalia, dorsal view (spermatheca shaded gray): 3, Selvadius nunenmacheri Gordon 1970 (Hyperaspidini: Selvadiina), showing distal end of sperm duct and spermatheca, accessory gland not shown (after Gordon 1985); 4, Erratodiomus brindisi Gordon 1999 (Hyperaspidini: Selvadiina), bursa through spermatheca, accessory gland not shown (after Gordon 1999); 5, Decadiomus hughesi Gordon &amp; Hilburn 1990 (Diomini), bursa through spermatheca (note long convoluted sperm duct); 6, M. lachesis (Diomini) (A.g.= accessory gland); 7–12, male genitalia of Diomini, left lateral view of penis: 7, D. hughesi; 8, M. lachesis; 9, Diomus donatus Gordon (capsule); 10, M. lachesis (capsule); 11, Decadiomus bigemmeus (capsule); 12, Decadiomus liebecki (capsule)

opennotspecifiedFeb 2019View details →
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FIGURES 1–2 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 1–2. Diagrammatic representation of major diagnostic features of Diomini and Hyperaspidini: 1, Diomini: a, ventral view of head capsule showing position of maxillary palp when retracted; b, left antennal club from dorsal view when extended; c, apex of mesothoracic leg showing trimerous tarsus; d, left half of first abdominal ventrite showing configuration of postcoxal line. 2, Hyperaspidini: a, ventral view of head capsule showing position of maxillary palp when retracted (left side of image) or extended (right side of image); b, left antennal club from dorsal view when extended (left image), same rotated 90 degrees counter clockwise to show membranous sensory patches of last two antennomeres (right image); c, apex of mesothoracic leg showing cryptotetramerous tarsus; d, left half of first abdominal ventrite showing various configurations of the postcoxal line.

opennotspecifiedFeb 2019View details →
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FIGURES 29–32 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 29–32. Male genitalia of Moiradiomus species (a, left lateral view of phallobase; b, ventral view of phallobase; c, left lateral view of penis; d, apex of basal lobe, enlarged): 29, M. clotho; 30, M. lachesis; 31, M. atopos; 32, M. nanita.

opennotspecifiedFeb 2019View details →
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FIGURES 40–42 in Overview of the lady beetle tribe Diomini (Coleoptera: Coccinellidae) and description of a new phytophagous, silk-spinning genus from Costa Rica that induces food bodies on leaves of Piper (Piperaceae)

FIGURES 40–42. Tents of Moiradiomus spp.: 40, M. lachesis on Piper lanosibracteum; 41, M. nanita on P. reticulatum; 42, M. atropos on P. friedrichsthalii.

opennotspecifiedFeb 2019View details →
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Food Security for an Aging and Heavier Population

<p>Supplementary Data Set&nbsp;</p> <p>The dataset include tables with population, and average food energy requirements, weight, height and age at the global and national levels from 1975 to 2014.</p> <p><br> Reference: &quot;V&aacute;squez, F., Vita, G. and M&uuml;ller, D. (2018) &lsquo;Food Security for an Aging and Heavier Population&rsquo;, Sustainability, 10(10), p. 3683. doi: 10.3390/su10103683.&quot;<br> &nbsp;</p>

opencc-by-4.0Oct 2018View details →
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FoodEx2vec: Poincaré Embeddings of a FoodEx2 Hierarchy for Advanced Food Data Analysis

<p>A dataset consisting of&nbsp;Poincar&eacute; embeddings of the FoodEx2 hierarchy, as well as the clustering results obtained with the&nbsp;Poincar&eacute; embeddings.</p> <p>It consists of two folders:</p> <ol> <li>foodex2vec_clusters - where the clustering using the Poincar&eacute; embeddings can be seen;</li> <li>foodex2vec_poincare_embeddings - the actual&nbsp;Poincar&eacute; embeddings with different dimensions.&nbsp;</li> </ol>

opencc-by-nc-sa-4.0Aug 2019View details →
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Supplementary material 1 from: Biscotti N, Bonsanto D, Viscio GD (2018) The traditional food use of wild vegetables in Apulia (Italy) in the light of Italian ethnobotanical literature. Italian Botanist 5: 1-24. https://doi.org/10.3897/italianbotanist.5.22297

Tables S1, S2, S3 : Explanation note: Table S1 (Learning areas divided by territorial district), Table S2 (Wild vegetables gathered and consumed in Apulia region) and Table S3 (Wild food plants of popular use in Italy by regions (Checklist)).

opencc-zeroOct 2019View details →
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FIGURES 1–6 in Immature stages of Neptis reducta Fruhstorfer, 1908 (Lepidoptera, Nymphalidae Neptini): morphology, ecology and food specialty

FIGURES 1–6. Specimens of Neptis species reared from Aphananthe aspera. 1–2. N. reducta ♂, TAIWAN: TAIZHONG CITY, Heping, Dongmaoshan, 800 m, X. 10. 2013, emgd. XII. 9. 2013 (13K7); 3–4. N. nata♂, TAIWAN: TAIZHONG CITY, Heping, Defulan Trail, ca 700 m, I. 22. 2013, emgd. II. 5. 2013 (13A12); 5–6 N. sappho♀, TAIWAN: MIAOLI Co., Taian, Xi- angbi, 750 m, XII. 1. 2012, emgd. XII. 23. 2012 (12M4). Scale bar = 1 cm.

opennotspecifiedOct 2019View details →
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FIGS. 13–18 in Immature stages of Neptis reducta Fruhstorfer, 1908 (Lepidoptera, Nymphalidae Neptini): morphology, ecology and food specialty

FIGS. 13–18. Pupae of Neptis species associated with Aphananthe aspera. 13–14. N. reducta; 15–16. N. nata; 17–18. N. sappho.

opennotspecifiedOct 2019View details →
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FIGS. 29–33 in Immature stages of Neptis reducta Fruhstorfer, 1908 (Lepidoptera, Nymphalidae Neptini): morphology, ecology and food specialty

FIGS. 29–33. Head capsules of Neptis sappho larvae. 29. 1st instar. 30. 2nd instar. 31. 3rd instar. 32. 4th instar. 33. 5th (final) instar. Scale bar = 200 μm for 29–30, 500 μm for 31–33.

opennotspecifiedOct 2019View details →
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FIGS. 19–23 in Immature stages of Neptis reducta Fruhstorfer, 1908 (Lepidoptera, Nymphalidae Neptini): morphology, ecology and food specialty

FIGS. 19–23. Head capsules of Neptis reducta larvae. 19. 1st instar. 20. 2nd instar. 21. 3rd instar. 22. 4th instar. 23. 5th (final) instar. Scale bar = 200 μm for 19–20, 500 μm for 11–23.

opennotspecifiedOct 2019View details →

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Allen Brain Atlas

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allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

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neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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